Schick33 100008636Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI D764100008636), received between Aug 10, 2023 and Apr 3, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Poor Quality Image” (3 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 3, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S1 STARTER KIT/3.0 INTERFACE 6', THEY ALLEGE EXPERIENCING CONNECTIVITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN OR AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24775650 ↗
• MalfunctionMar 23, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S1 STARTER KIT/3.0 INTERFACE 6', THEY ALLEGE THERE WAS AN X-RAY IMAGE TRANSMISSION ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (TRANSMISSION FAILURE). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24661792 ↗
• MalfunctionFeb 24, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S1 STARTER KIT/3.0 INTERFACE 6', THEY ALLEGE EXPERIENCING CONNECTIVITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN OR AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24430893 ↗
• MalfunctionAug 10, 2023Image Display Error/Artifact; Image Display Error/Artifact

  WHILE USING A SCHICK 33 SENSOR INTRAORAL X-RAY UNIT, AN INCORRECT IMAGE WAS DISPLAYED DURING USE. THIS WAS IMMEDIATELY NOTICEABLE TO THE CLINICIAN AND NO INJURY RESULTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17503121 ↗